Akira Itoh

Dr. Akira Itoh

orcid

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 February 2022 in New Phytologist
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Journal Article
Closed access
CPCamille Piponiot
Camille Piponiot
KAKristina J. Anderson‐Teixeira
Kristina J. Anderson‐Teixeira
SDStuart J. Davies
Stuart J. Davies
DADavid Allen
David Allen
NBNorman A. Bourg
Norman A. Bourg
HMHelene C. Muller‐Landau
Helene C. Muller‐Landau

7 May 2003 in Ecological Research
Verified
Journal Article
Closed access
PDF file
AIAkira Itoh
Akira Itoh
TYTakuo Yamakura
Takuo Yamakura
TOTatsuhiro Ohkubo
Tatsuhiro Ohkubo
MKMamoru Kanzaki
Mamoru Kanzaki
PPPeter A. Palmiotto
Peter A. Palmiotto
HLHua Seng Lee
Hua Seng Lee

20 May 2020 in New Phytologist
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Journal Article
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MWMonique Weemstra
Monique Weemstra
KPKabir Peay
Kabir Peay
SDStuart J. Davies
Stuart J. Davies
MMMohizah Mohamad
Mohizah Mohamad
AIAkira Itoh
Akira Itoh
SRSabrina E Russo
Sabrina E Russo

28 February 2024 in Nature
Verified
Journal Article
Open access
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LHLisa Hülsmann
Lisa Hülsmann
RCRyan A. Chisholm
Ryan A. Chisholm
LCLiza Comita
Liza Comita
MVMarco D. Visser
Marco D. Visser
MLMelina de Souza Leite
Melina de Souza Leite
FHFlorian Hartig
Florian Hartig
Numerous studies have shown reduced performance in plants that are surrounded by neighbours of the same species1,2, a phenomenon known as conspecific negative density dependence (CNDD)3. A long-held ecological hypothesis posits that CNDD is more pronounced in tropical than in temperate forests4,5, which increases community stabilization, species coexistence and the diversity of local tree species6,7. Previous analyses supporting such a latitudinal gradient in CNDD8,9 have suffered from methodological limitations related to the use of static data10–12. Here we present a comprehensive assessment of latitudinal CNDD patterns using dynamic mortality data to estimate species-site-specific CNDD across 23 sites. Averaged across species, we found that stabilizing CNDD was present at all except one site, but that average stabilizing CNDD was not stronger toward the tropics. However, in tropical tree communities, rare and intermediate abundant species experienced stronger stabilizing CNDD than did common species. This pattern was absent in temperate forests, which suggests that CNDD influences species abundances more strongly in tropical forests than it does in temperate ones13. We also found that interspecific variation in CNDD, which might attenuate its stabilizing effect on species diversity14,15, was high but not significantly different across latitudes. Although the consequences of these patterns for latitudinal diversity gradients are difficult to evaluate, we speculate that a more effective regulation of population abundances could translate into greater stabilization of tropical tree communities and thus contribute to the high local diversity of tropical forests.

17 May 2012 in Biotropica
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Journal Article
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AIAkira Itoh
Akira Itoh
SNSatoshi Nanami
Satoshi Nanami
THTsuyoshi Harata
Tsuyoshi Harata
TOTatsuhiro Ohkubo
Tatsuhiro Ohkubo
STSylvester Tan
Sylvester Tan
TYTakuo Yamakura
Takuo Yamakura

12 May 2022 in Journal of Ecology
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Journal Article
Open access
SKStephan Kambach
Stephan Kambach
RCRichard Condit
Richard Condit
SASalomón Aguilar
Salomón Aguilar
HBHelge Bruelheide
Helge Bruelheide
SBSarayudh Bunyavejchewin
Sarayudh Bunyavejchewin
NRNadja Rüger
Nadja Rüger
Organisms of all species must balance their allocation to growth, survival and recruitment. Among tree species, evolution has resulted in different life‐history strategies for partitioning resources to these key demographic processes. Life‐history strategies in tropical forests have often been shown to align along a trade‐off between fast growth and high survival, that is, the well‐known fast–slow continuum. In addition, an orthogonal trade‐off has been proposed between tall stature—resulting from fast growth and high survival—and recruitment success, that is, a stature−recruitment trade‐off. However, it is not clear whether these two independent dimensions of life‐history variation structure tropical forests worldwide. We used data from 13 large‐scale and long‐term tropical forest monitoring plots in three continents to explore the principal trade‐offs in annual growth, survival and recruitment as well as tree stature. These forests included relatively undisturbed forests as well as typhoon‐disturbed forests. Life‐history variation in 12 forests was structured by two orthogonal trade‐offs, the growth−survival trade‐off and the stature−recruitment trade‐off. Pairwise Procrustes analysis revealed a high similarity of demographic relationships among forests. The small deviations were related to differences between African and Asian plots. Synthesis. The fast–slow continuum and tree stature are two independent dimensions structuring many, but not all tropical tree communities. Our discovery of the consistency of demographic trade‐offs and life‐history strategies across different forest types from three continents substantially improves our ability to predict tropical forest dynamics worldwide.